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寨卡病毒的核苷类似物抑制剂

Nucleoside Inhibitors of Zika Virus.

作者信息

Eyer Luděk, Nencka Radim, Huvarová Ivana, Palus Martin, Joao Alves Maria, Gould Ernest A, De Clercq Erik, Růžek Daniel

机构信息

Department of Virology, Veterinary Research Institute, Brno.

Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague.

出版信息

J Infect Dis. 2016 Sep 1;214(5):707-11. doi: 10.1093/infdis/jiw226. Epub 2016 May 27.

Abstract

There is growing evidence that Zika virus (ZIKV) can cause devastating infant brain defects and other neurological disorders in humans. However, no specific antiviral therapy is available at present. We tested a series of 2'-C- or 2'-O-methyl-substituted nucleosides, 2'-C-fluoro-2'-C-methyl-substituted nucleosides, 3'-O-methyl-substituted nucleosides, 3'-deoxynucleosides, derivatives with 4'-C-azido substitution, heterobase-modified nucleosides, and neplanocins for their ability to inhibit ZIKV replication in cell culture. Antiviral activity was identified when 2'-C-methylated nucleosides were tested, suggesting that these compounds might represent promising lead candidates for further development of specific antivirals against ZIKV.

摘要

越来越多的证据表明,寨卡病毒(ZIKV)可导致人类婴儿出现严重的脑部缺陷和其他神经疾病。然而,目前尚无特异性抗病毒疗法。我们测试了一系列2'-C-或2'-O-甲基取代核苷、2'-C-氟-2'-C-甲基取代核苷、3'-O-甲基取代核苷、3'-脱氧核苷、具有4'-C-叠氮取代的衍生物、杂碱基修饰核苷以及杀稻瘟菌素抑制ZIKV在细胞培养中复制的能力。在测试2'-C-甲基化核苷时发现了抗病毒活性,这表明这些化合物可能是进一步开发针对ZIKV的特异性抗病毒药物的有前景的先导候选物。

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